510(k) K080171 ยท KNW Instrument, Biopsy
SANARUS INCORE ROTATIONAL CORE BIOPSY DEVICE, MODELS CB3010, CB3012
| Applicant | Sanarus Medical, Inc., Pleasanton CA, US |
| Decision | Substantially Equivalent, Mar 6, 2008 |
| Received | Jan 24, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K080171
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.